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Efficacy and Safety of Abelmoschus Manihot for Diabetic Kidney Disease: a Randomized, Multicenter, Positive-Drug Parallel Controlled Clinical Trial

Efficacy and Safety of Abelmoschus Manihot for Diabetic Kidney Disease: a Randomized, Multicenter, Positive-Drug Parallel Controlled Clinical Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025273
Enrollment
Unknown
Registered
2019-08-20
Start date
2019-12-16
Completion date
Unknown
Last updated
2025-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Kidney Disease

Interventions

losartan potassium:100mg / dose, 1 time / day, orally after meals
Abelmoschus manihot:2.5g / dose, 3 times / day, orally after meals

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diabetes diagnosis; 2. Diabetic Kidney Disease III periody diagnosis (two positive results out of examinations on three different days); 3. Aged 18-75 years, no gender specified; 4. Blood pressure effectively controlled = 60mL/min; 6. HbA1c <= 9%; 7. Informed consent signed.

Exclusion criteria

Exclusion criteria: 1. Known non-diabetes secondary renal disease; 2. History of Abelmoschus Manihot,ACEI and/or ARB drugs within 1 month prior to enrollment; 3. History of glucocorticoids, immunosuppressive agents or Tripterygium Wilfordii Hook F (TwHF) within 1 month prior to enrollment; 4. Unstable angina pectoris, myocardial infarction and/or coronary stent implantation within 3 months; 5. Liver failure and/or history of hepatic encephalopathy; 6. Malignant tumors or malignant diseases that affect overall prognosis; 7. Triglyceride >= 5.7mmol/L; 8. Pregnancy and lactation; 9. Allergy to losartan potassium or Abelmoschus Manihot; 10. History of unilateral or bilateral renal artery stenosis; 11. Blood pressure < 90/60mmHg; 12. Alcohol or drug use; 13. Participation in other clinical research.

Design outcomes

Primary

MeasureTime frame
ACR;

Secondary

MeasureTime frame
eGFR;hs-CRP;

Countries

China

Contacts

Public ContactWeiping Jia

Shanghai Sixth People's Hospital

wpjia@yahoo.com+86 13818888939

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026